IDENTITY OF PROSTATE SPECIFIC ANTIGEN AND THE SEMEN PROTEIN-P-30 PURIFIED BY A RAPID CHROMATOGRAPHY TECHNIQUE

被引:52
作者
GRAVES, HCB
KAMAREI, M
STAMEY, TA
机构
[1] Urology S287, Stanford University, Medical Center, Stanford, CA 94305
关键词
D O I
10.1016/S0022-5347(17)39788-4
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Previous investigators have reported the identity of prostate specific antigen (PSA) and the semen protein p30, but data to support these claims have not been published. We report here the rapid and continuous purification of PSA using a simple two column chromatography technique originally developed for purification of p30. Using commercial antisera to PSA and original antisera to p30 for detection, we show that the two glycoproteins have identical purification profiles by this technique which uses cation exchange chromatography and sizing chromatography. The antigens also have identical molecular weights by gel electrophoresis and gel filtration. Furthermore, both antigens correspond to the same prominent protein band in seminal plasma by sodium dodecylsulfate polyacrylamide gel electrophoresis. On commercial immunoassay for PSA, purified p30 gives a calibration curve identical to the commercial PSA kit calibrator (Pros-check(TM) PSA Radioimmunoassay, Yang Laboratories). We conclude that PSA and the semen protein p30 are identical and can be easily purified by a rapid continuous technique.
引用
收藏
页码:1510 / 1515
页数:6
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